ENST00000342992.11:c.96661G>C
(TTN)
|
ENSP00000343764.6:p.Glu32221Gln
|
|
ENST00000342175.11:c.77746G>C
(TTN)
|
ENSP00000340554.6:p.Glu25916Gln
|
|
ENST00000359218.10:c.77545G>C
(TTN)
|
ENSP00000352154.5:p.Glu25849Gln
|
|
ENST00000342175.10:c.77746G>C
(TTN)
|
ENSP00000340554.6:p.Glu25916Gln
|
|
ENST00000342992.10:c.96661G>C
(TTN)
|
ENSP00000343764.6:p.Glu32221Gln
|
|
ENST00000359218.9:c.77545G>C
(TTN)
|
ENSP00000352154.5:p.Glu25849Gln
|
|
ENST00000460472.6:c.77170G>C
(TTN)
|
ENSP00000434586.1:p.Glu25724Gln
|
|
ENST00000589042.5:c.104365G>C
(TTN)
MANE Select
|
ENSP00000467141.1:p.Glu34789Gln
|
|
ENST00000591111.5:c.99442G>C
(TTN)
|
ENSP00000465570.1:p.Glu33148Gln
|
|
ENST00000615779.4:c.99442G>C
(TTN)
|
ENSP00000483597.1:p.Glu33148Gln
|
|
NM_001256850.1:c.99442G>C
(TTN)
|
NP_001243779.1:p.Glu33148Gln
|
|
NM_001267550.2:c.104365G>C
(TTN)
MANE Select
|
NP_001254479.2:p.Glu34789Gln
|
|
NM_003319.4:c.77170G>C
(TTN)
|
NP_003310.4:p.Glu25724Gln
|
|
NM_133378.4:c.96661G>C
(TTN)
|
NP_596869.4:p.Glu32221Gln
|
|
NM_133432.3:c.77545G>C
(TTN)
|
NP_597676.3:p.Glu25849Gln
|
|
NM_133437.4:c.77746G>C
(TTN)
|
NP_597681.4:p.Glu25916Gln
|
|
NR_038271.1:n.446+8614C>G
(TTN-AS1)
|
|
|
NR_038272.1:n.220-3482C>G
(TTN-AS1)
|
|
|
XM_011511729.1:c.103462G>C
(TTN)
|
XP_011510031.1:p.Glu34488Gln
|
|
XM_011511730.1:c.77356G>C
(TTN)
|
XP_011510032.1:p.Glu25786Gln
|
|
XM_011511731.1:c.77215G>C
(TTN)
|
XP_011510033.1:p.Glu25739Gln
|
|
XM_017004819.1:c.103258G>C
(TTN)
|
XP_016860308.1:p.Glu34420Gln
|
|
XM_017004820.1:c.98656G>C
(TTN)
|
XP_016860309.1:p.Glu32886Gln
|
|
XM_017004821.1:c.98653G>C
(TTN)
|
XP_016860310.1:p.Glu32885Gln
|
|
XM_017004822.1:c.95695G>C
(TTN)
|
XP_016860311.1:p.Glu31899Gln
|
|
XM_017004823.1:c.77311G>C
(TTN)
|
XP_016860312.1:p.Glu25771Gln
|
|
XM_024453094.1:c.98806G>C
(TTN)
|
XP_024308862.1:p.Glu32936Gln
|
|
XM_024453095.1:c.98803G>C
(TTN)
|
XP_024308863.1:p.Glu32935Gln
|
|
XM_024453096.1:c.98236G>C
(TTN)
|
XP_024308864.1:p.Glu32746Gln
|
|
XM_024453097.1:c.95578G>C
(TTN)
|
XP_024308865.1:p.Glu31860Gln
|
|
XM_024453098.1:c.95497G>C
(TTN)
|
XP_024308866.1:p.Glu31833Gln
|
|
XM_024453099.1:c.77260G>C
(TTN)
|
XP_024308867.1:p.Glu25754Gln
|
|
XM_024453100.1:c.67114G>C
(TTN)
|
XP_024308868.1:p.Glu22372Gln
|
|